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183 Possible Causes for MYO1A,, SER910PRO

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  • Deafness, Autosomal Dominant 23

    FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, GRHL2, GRIN2A, HGF, HOMER2, ILDR1, KARS, KCNJ10, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MSRB3, MYH14, MYH9, MYO1A[bredagenetics.com] HSA: 6495 ] [KO: K15614 ] SLC17A8 [HSA: 246213 ] [KO: K12302 ] GRHL2 [HSA: 79977 ] [KO: K09275 ] TMC1 [HSA: 117531 ] [KO: K21988 ] DSPP [HSA: 1834 ] CCDC50 [HSA: 152137 ] MYO1A[genome.jp] Genes Sampled DFNA : ACTB , CCDC50 , CEACAM16 , COCH , CRYM , ICERE1 , DIABLO , DIAPH1 , DSPP , EYA4 , GJB3 , GRHL2 , HOMER2 , KCNQ4 , KITLG , MCM2 , miR96 , MYH14 , MYH9 , MYO1A[otogenetics.com]

    Missing: SER910PRO
  • Autosomal Dominant Deafness 28

    Third, a nonsense mutation was found in exon 4 of MYO1A in the proband of Newfoundland Family 2102.[research.library.mun.ca] HSA: 6495 ] [KO: K15614 ] SLC17A8 [HSA: 246213 ] [KO: K12302 ] GRHL2 [HSA: 79977 ] [KO: K09275 ] TMC1 [HSA: 117531 ] [KO: K21988 ] DSPP [HSA: 1834 ] CCDC50 [HSA: 152137 ] MYO1A[genome.jp] HOMER2 , HSD17B4 , ILDR1 , KARS , KCNE1 , KCNJ10 , KCNQ1 , KCNQ4 , LARS2 , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MASP1 , MITF , MSRB3 , MT-RNR1 , MYH14 , MYH9 , MYO15A , MYO1A[egl-eurofins.com]

    Missing: SER910PRO
  • Mitochondrial Non-Syndromic Sensorineural Deafness

    FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, GRHL2, GRIN2A, HGF, HOMER2, ILDR1, KARS, KCNJ10, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MSRB3, MYH14, MYH9, MYO1A[bredagenetics.com] The GJB3 and MYO1A genes are associated with nonsyndromic deafness. The causes of nonsyndromic deafness are complex.[ourmed.org] HOMER2 , HSD17B4 , ILDR1 , KARS , KCNE1 , KCNJ10 , KCNQ1 , KCNQ4 , LARS2 , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MASP1 , MITF , MSRB3 , MT-RNR1 , MYH14 , MYH9 , MYO15A , MYO1A[egl-eurofins.com]

    Missing: SER910PRO
  • X-Linked Non-Syndromic Sensorineural Deafness Type DFN

    FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, GRHL2, GRIN2A, HGF, HOMER2, ILDR1, KARS, KCNJ10, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MSRB3, MYH14, MYH9, MYO1A[bredagenetics.com] The GJB3 and MYO1A genes are associated with nonsyndromic deafness. The causes of nonsyndromic deafness are complex.[ourmed.org] […] with weaker evidence currently implicating genes CCDC50 , DIAPH1 , DSPP , ESRRB , GJB3 , GRHL2 , GRXCR1 , HGF , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MIR96 , MYH14 , MYH9 , MYO1A[en.wikipedia.org]

    Missing: SER910PRO
  • Autosomal Recessive Deafness 24

    FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, GRHL2, GRIN2A, HGF, HOMER2, ILDR1, KARS, KCNJ10, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MSRB3, MYH14, MYH9, MYO1A[bredagenetics.com] HOMER2 , HSD17B4 , ILDR1 , KARS , KCNE1 , KCNJ10 , KCNQ1 , KCNQ4 , LARS2 , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MASP1 , MITF , MSRB3 , MT-RNR1 , MYH14 , MYH9 , MYO15A , MYO1A[egl-eurofins.com] […] with weaker evidence currently implicating genes CCDC50 , DIAPH1 , DSPP , ESRRB , GJB3 , GRHL2 , GRXCR1 , HGF , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MIR96 , MYH14 , MYH9 , MYO1A[en.wikipedia.org]

    Missing: SER910PRO
  • Autosomal Dominant Deafness 11

    FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, GRHL2, GRIN2A, HGF, HOMER2, ILDR1, KARS, KCNJ10, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MSRB3, MYH14, MYH9, MYO1A[bredagenetics.com] Genes Sampled DFNA : ACTB , CCDC50 , CEACAM16 , COCH , CRYM , ICERE1 , DIABLO , DIAPH1 , DSPP , EYA4 , GJB3 , GRHL2 , HOMER2 , KCNQ4 , KITLG , MCM2 , miR96 , MYH14 , MYH9 , MYO1A[otogenetics.com] […] with weaker evidence currently implicating genes CCDC50 , DIAPH1 , DSPP , ESRRB , GJB3 , GRHL2 , GRXCR1 , HGF , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MIR96 , MYH14 , MYH9 , MYO1A[ipfs.io]

    Missing: SER910PRO
  • Autosomal Recessive Deafness 42

    HOMER2 , HSD17B4 , ILDR1 , KARS , KCNE1 , KCNJ10 , KCNQ1 , KCNQ4 , LARS2 , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MASP1 , MITF , MSRB3 , MT-RNR1 , MYH14 , MYH9 , MYO15A , MYO1A[egl-eurofins.com] […] with weaker evidence currently implicating genes CCDC50 , DIAPH1 , DSPP , ESRRB , GJB3 , GRHL2 , GRXCR1 , HGF , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MIR96 , MYH14 , MYH9 , MYO1A[en.wikipedia.org] […] polypeptide 14 MYH14 DFNA4 608568 23212 myosin heavy chain 9 myosin, heavy chain 9, non-muscle myosin, heavy polypeptide 9, non-muscle MYH9 DFNA17 160775 7579 myosin IA MYO1A[ukgtn.nhs.uk]

    Missing: SER910PRO
  • Autosomal Recessive Deafness 44

    HOMER2 , HSD17B4 , ILDR1 , KARS , KCNE1 , KCNJ10 , KCNQ1 , KCNQ4 , LARS2 , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MASP1 , MITF , MSRB3 , MT-RNR1 , MYH14 , MYH9 , MYO15A , MYO1A[egl-eurofins.com] […] with weaker evidence currently implicating genes CCDC50 , DIAPH1 , DSPP , ESRRB , GJB3 , GRHL2 , GRXCR1 , HGF , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MIR96 , MYH14 , MYH9 , MYO1A[en.wikipedia.org] […] polypeptide 14 MYH14 DFNA4 608568 23212 myosin heavy chain 9 myosin, heavy chain 9, non-muscle myosin, heavy polypeptide 9, non-muscle MYH9 DFNA17 160775 7579 myosin IA MYO1A[ukgtn.nhs.uk]

    Missing: SER910PRO
  • Hypochondrogenesis

    […] geenejä kromosomissa 12: COL2A1: α-ketjun tyypin II kollageenia; HPD: 4-hydroksifenyylipyruvaatti dioksygenaasi; MMAB: liittyvät geenin all'aciduria metyylimalonihappoa; MYO1A[tallanopsis.com] […] identificerede gener på kromosom 12: COL2A1: α-kæden af collagen type II; HPD: 4-hydroxyfenylpyruvatdioxygenase; MMAB: relaterede gen all'aciduria methylmalonsyresænkende; MYO1A[articodore.com] Macrothrombocytopenia and progressive sensorineural deafness, May-Hegglin anomaly, Sebastian syndrome MYH14 Deafness, Peripheral neuropathy, myopathy, hoarseness, and hearing loss MYO1A[genda.com.ar]

    Missing: SER910PRO
  • Autosomal Recessive Deafness 1B

    FOXI1, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, GRHL2, GRIN2A, HGF, HOMER2, ILDR1, KARS, KCNJ10, KCNQ4, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MET, MIR96, MSRB3, MYH14, MYH9, MYO1A[bredagenetics.com] […] with weaker evidence currently implicating genes CCDC50 , DIAPH1 , DSPP , ESRRB , GJB3 , GRHL2 , GRXCR1 , HGF , LHFPL5 , LOXHD1 , LRTOMT , MARVELD2 , MIR96 , MYH14 , MYH9 , MYO1A[en.wikipedia.org] […] polypeptide 14 MYH14 DFNA4 608568 23212 myosin heavy chain 9 myosin, heavy chain 9, non-muscle myosin, heavy polypeptide 9, non-muscle MYH9 DFNA17 160775 7579 myosin IA MYO1A[ukgtn.nhs.uk]

    Missing: SER910PRO

Further symptoms